5-((4-Chlorophenyl)thio)-N-propyl-1,2,3-thiadiazole-4-carboxamide CAS 303151-50-0

Purity 97%+In StockPharmaceutical Standards
CAS No.303151-50-0
Molecular FormulaC12H12ClN3OS2
Molecular Weight313.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-((4-Chlorophenyl)thio)-N-propyl-1,2,3-thiadiazole-4-carboxamide CAS 303151-50-0 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO supplies 5-((4-Chlorophenyl)thio)-N-propyl-1,2,3-thiadiazole-4-carboxamide (CAS 303151-50-0), a certified reference material (molecular formula C12H12ClN3OS2, MW 313.83 g/mol) for analytical method development and quality control.

5-((4-Chlorophenyl)thio)-N-propyl-1,2,3-thiadiazole-4-carboxamide (C12H12ClN3OS2) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

As a certified reference material (CRM), 5-((4-Chlorophenyl)thio)-N-propyl-1,2,3-thiadiazole-4-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H12ClN3OS2
Molecular Weight313.83 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms2

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